Elalouf Ofir, Elkayam Ori
Department of Rheumatology, Tel Aviv Medical Center.
Harefuah. 2017 Jul;156(7):451-454.
Rheumatoid arthritis affects around 1% of the population. The disease is characterized by joint inflammation and damage. Therapy with disease modifying drugs (DMARDs) has been proved to be efficient in decreasing disease activity and progress, along with improvement in symptoms and prevention of structural damage. The sooner the therapy is initiated, the better the outcome, probably due to a decreased burden of inflammation. The therapeutic potential of early treatment led to an accelerating interest in the preclinical phase of the disease. Many studies demonstrated that there is a preclinical period that precedes the development of clinical arthritis, and the old assumption that the disease develops with the clinical symptoms is no longer valid. Apparently, many biological markers, including autoantibodies, appear years before the clinical synovitis develops. This period is called preclinical rheumatoid arthritis. In the preclinical phase, autoantibodies such as rheumatoid factor, antibodies to citrullinated proteins and many other antibodies and inflammatory markers are abundant. These findings and the evidence of genetic and environmental risk factors for rheumatoid arthritis support the theory which claims that multiple factors contribute to the development of an autoimmune process that progresses and expands until reaching a critical point where rheumatoid arthritis develops.
类风湿关节炎影响着约1%的人口。该疾病的特征是关节炎症和损伤。使用改善病情抗风湿药(DMARDs)进行治疗已被证明在降低疾病活动度和进展、改善症状以及预防结构损伤方面是有效的。治疗开始得越早,效果越好,这可能是由于炎症负担减轻。早期治疗的潜在疗效引发了对该疾病临床前期的兴趣加速增长。许多研究表明,在临床关节炎出现之前存在一个临床前期,并且疾病随临床症状发展的旧有假设已不再成立。显然,包括自身抗体在内的许多生物标志物在临床滑膜炎出现前数年就已出现。这个时期被称为临床前期类风湿关节炎。在临床前期阶段,类风湿因子、抗瓜氨酸化蛋白抗体以及许多其他抗体和炎症标志物等自身抗体大量存在。这些发现以及类风湿关节炎的遗传和环境危险因素的证据支持了这样一种理论,即多种因素促成了自身免疫过程的发展,该过程不断进展和扩展,直至达到类风湿关节炎发病的临界点。